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Structural signature of SCA3: From presymptomatic to late disease stages

Annals of neurology, 2018-09, Vol.84 (3), p.401-408

2018

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Quantitative ultrasonography reveals skeletal muscle abnormalities in carriers of DMD pathogenic variants

Muscle & nerve, 2024-06, Vol.69 (6), p.682-690

2024

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A‐waves are associated with neuropathic pain in leprosy

Muscle & nerve, 2023-02, Vol.67 (2), p.165-168

2023

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A healthcare claims analysis to identify and characterize patients with suspected X-Linked Myotubular Myopathy (XLMTM) in the Brazilian Healthcare System

Orphanet journal of rare diseases, 2024-05, Vol.19 (1), p.188-188, Article 188

2024

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MicroRNAs-424 and 206 are potential prognostic markers in spinal onset amyotrophic lateral sclerosis

Journal of the neurological sciences, 2016-09, Vol.368, p.19-24

2016

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Tract‐Specific Spinal Cord Diffusion Tensor Imaging in Friedreich's Ataxia

Movement disorders, 2022-02, Vol.37 (2), p.354-364

2022

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Pre-clinical left ventricular myocardial remodeling in patients with Friedreich's ataxia: A cardiac MRI study

PloS one, 2021-03, Vol.16 (3), p.e0246633-e0246633

2021

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A multimodal evaluation of microstructural white matter damage in spinocerebellar ataxia type 3

Movement disorders, 2013-07, Vol.28 (8), p.1125-1132

2013

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Brain Damage and Gene Expression Across Hereditary Spastic Paraplegia Subtypes

Movement disorders, 2021-07, Vol.36 (7), p.1644-1653

2021

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Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis

Journal of neurology, neurosurgery and psychiatry, 2024-02, Vol.95 (2), p.103-113

2024

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Clinical Neurophysiology of Zika Virus-Related Disorders of the Peripheral Nervous System in Adults

Journal of clinical neurophysiology, 2022-05, Vol.39 (4), p.253-258

2022

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Clinical Neurophysiology of Zika Virus Infection

Journal of clinical neurophysiology, 2022-05, Vol.39 (4), p.247-247

2022

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Amyotrophic lateral sclerosis type 8 is not a pure motor disease: evidence from a neuropsychological and behavioural study

Journal of neurology, 2019-08, Vol.266 (8), p.1980-1987

2019

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Gluten Ataxia: an Overestimated Condition?

Cerebellum (London, England), 2022-08, Vol.21 (4), p.617-619

2022

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Randomized Trial of Botulinum Toxin Type A in Hereditary Spastic Paraplegia — The SPASTOX Trial

Movement disorders, 2021-07, Vol.36 (7), p.1654-1663

2021

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Language impairment in sporadic and familial (type 8) amyotrophic lateral sclerosis: A comparative study

Muscle & nerve, 2024-07, Vol.70 (1), p.130-139

2024

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Laryngeal electromyography in amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2020-07, Vol.91 (7), p.730-732

2020

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Genetic epidemiology of familial ALS in Brazil

Neurobiology of aging, 2021-06, Vol.102, p.227.e1-227.e4

2021

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Retinal Architecture in Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (ARSACS): Insights into Disease Pathogenesis and Biomarkers

Movement disorders, 2021-09, Vol.36 (9), p.2027-2035

2021

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Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study

Journal of neurology, neurosurgery and psychiatry, 2024-02, Vol.95 (7), p.682-690

2024

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Advanced Structural Magnetic Resonance Imaging of the Spinal Cord: Technical Aspects and Clinical Use

Seminars in ultrasound, CT, and MRI, 2023-10, Vol.44 (5), p.464-468

2023

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Movement disorders in hereditary spastic paraplegias

Arquivos de neuro-psiquiatria, 2023-11, Vol.81 (11), p.1000-1007

2023

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The Role of MRI in the Diagnosis of Spinal Cord Tumors

Seminars in ultrasound, CT, and MRI, 2023-10, Vol.44 (5), p.436-451

2023

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Exploratory structural assessment in craniocervical dystonia: Global and differential analyses

PloS one, 2017-08, Vol.12 (8), p.e0182735-e0182735

2017

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Progression of ataxia in patients with Machado-Joseph disease

Movement disorders, 2009-07, Vol.24 (9), p.1387-1390

2009

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Structural signature of SCA3: From presymptomatic to late disease stages

Quantitative ultrasonography reveals skeletal muscle abnormalities in carriers of DMD pathogenic variants

A‐waves are associated with neuropathic pain in leprosy

A healthcare claims analysis to identify and characterize patients with suspected X-Linked Myotubular Myopathy (XLMTM) in the Brazilian Healthcare System

MicroRNAs-424 and 206 are potential prognostic markers in spinal onset amyotrophic lateral sclerosis

Tract‐Specific Spinal Cord Diffusion Tensor Imaging in Friedreich's Ataxia

Pre-clinical left ventricular myocardial remodeling in patients with Friedreich's ataxia: A cardiac MRI study

A multimodal evaluation of microstructural white matter damage in spinocerebellar ataxia type 3

Brain Damage and Gene Expression Across Hereditary Spastic Paraplegia Subtypes

Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis

Clinical Neurophysiology of Zika Virus-Related Disorders of the Peripheral Nervous System in Adults

Clinical Neurophysiology of Zika Virus Infection

Amyotrophic lateral sclerosis type 8 is not a pure motor disease: evidence from a neuropsychological and behavioural study

Gluten Ataxia: an Overestimated Condition?

Randomized Trial of Botulinum Toxin Type A in Hereditary Spastic Paraplegia — The SPASTOX Trial

Language impairment in sporadic and familial (type 8) amyotrophic lateral sclerosis: A comparative study

Laryngeal electromyography in amyotrophic lateral sclerosis

Genetic epidemiology of familial ALS in Brazil

Retinal Architecture in Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (ARSACS): Insights into Disease Pathogenesis and Biomarkers

Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study

Advanced Structural Magnetic Resonance Imaging of the Spinal Cord: Technical Aspects and Clinical Use

Movement disorders in hereditary spastic paraplegias

The Role of MRI in the Diagnosis of Spinal Cord Tumors

Exploratory structural assessment in craniocervical dystonia: Global and differential analyses

Progression of ataxia in patients with Machado-Joseph disease

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